Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

Por Kaplan, Michael, Renbaum, Paul, Levy-Lahad, Ephrat, Hammerman, Cathy, Lahad, Amnon, Beutler, Ernest
Publicado em 1997

Prenatal Isolated Ventricular Septal Defect May Not Be Associated with Trisomy 21

Por Shen, Ori, Lieberman, Sari, Farber, Benjamin, Terner, Daniel, Lahad, Amnon, Levy-Lahad, Ephrat
Publicado no J Clin Med (2014)

Why should primary care physicians know about breast cancer genetics?

Por Pinsky, Linda E, Culver, Julie Bars, Hull, Judith, Levy-Lahad, Ephrat, Daly, Mary, Burke, Wylie
Publicado em 2001

VRK1 regulates Cajal body dynamics and protects coilin from proteasomal degradation in cell cycle

Por Cantarero, Lara, Sanz-García, Marta, Vinograd-Byk, Hadar, Renbaum, Paul, Levy-Lahad, Ephrat, Lazo, Pedro A.
Publicado no Sci Rep (2015)

Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene

Por Renbaum, Paul, Kellerman, Efrat, Jaron, Ranit, Geiger, Dan, Segel, Reeval, Lee, Ming, King, Mary Claire, Levy-Lahad, Ephrat
Publicado em 2009

Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy

Por Altarescu, Gheona, Eldar-Geva, Talia, Brooks, Baruch, Zylber-Haran, Edith, Varshaver, Irit, Margalioth, Ehud J., Levy-Lahad, Ephrat, Renbaum, Paul
Publicado em 2009

High school Tay–Sachs disease carrier screening: 5 to 11-year follow-up

Por Curd, Helen, Lewis, Sharon, Macciocca, Ivan, Sahhar, Margaret, Petrou, Vicki, Bankier, Agnes, Lieberman, Sari, Levy-Lahad, Ephrat, Delatycki, Martin B.
Publicado em 2013

Preimplantation genetic diagnosis (PGD) for SHOX-related haploinsufficiency in conjunction with trisomy 21 detection by molecular analysis

Por Altarescu, Gheona, Reish, Orit, Renbaum, Paul, Kasterstein, Ester, Komarovsky, Dvorah, Komsky, Alisa, Bern, Orna, Strassburger, Dvorah, Levy-Lahad, Ephrat, Ron-El, Raphael
Publicado em 2010

Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

Por Toperoff, Gidon, Aran, Dvir, Kark, Jeremy D., Rosenberg, Michael, Dubnikov, Tatyana, Nissan, Batel, Wainstein, Julio, Friedlander, Yechiel, Levy-Lahad, Ephrat, Glaser, Benjamin, Hellman, Asaf
Publicado em 2012

Prevention of Lysosomal Storage Diseases and Derivation of Mutant Stem Cell Lines by Preimplantation Genetic Diagnosis

Por Altarescu, Gheona, Beeri, Rachel, Eiges, Rachel, Epsztejn-Litman, Silvina, Eldar-Geva, Talia, Elstein, Deborah, Zimran, Ari, Margalioth, Ehud J., Levy-Lahad, Ephrat, Renbaum, Paul
Publicado em 2012

Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome

Por Pierce, Sarah B., Gersak, Ksenija, Michaelson-Cohen, Rachel, Walsh, Tom, Lee, Ming K., Malach, Daniel, Klevit, Rachel E., King, Mary-Claire, Levy-Lahad, Ephrat
Publicado em 2013

TODRA, a lncRNA at the RAD51 Locus, Is Oppositely Regulated to RAD51, and Enhances RAD51-Dependent DSB (Double Strand Break) Repair

Por Gazy, Inbal, Zeevi, David A., Renbaum, Paul, Zeligson, Sharon, Eini, Lital, Bashari, Dana, Smith, Yoav, Lahad, Amnon, Goldberg, Michal, Ginsberg, Doron, Levy-Lahad, Ephrat
Publicado no PLoS One (2015)

Establishment of Homozygote Mutant Human Embryonic Stem Cells by Parthenogenesis

Por Epsztejn-Litman, Silvina, Cohen-Hadad, Yaara, Aharoni, Shira, Altarescu, Gheona, Renbaum, Paul, Levy-Lahad, Ephrat, Schonberger, Oshrat, Eldar-Geva, Talia, Zeligson, Sharon, Eiges, Rachel
Publicado no PLoS One (2015)

Snord 3A: A Molecular Marker and Modulator of Prion Disease Progression

Por Cohen, Eran, Avrahami, Dana, Frid, Kati, Canello, Tamar, Levy Lahad, Ephrat, Zeligson, Sharon, Perlberg, Shira, Chapman, Joab, Cohen, Oren S., Kahana, Esther, Lavon, Iris, Gabizon, Ruth
Publicado em 2013

Testicular differentiation factor SF-1 is required for human spleen development

Por Zangen, David, Kaufman, Yotam, Banne, Ehud, Weinberg-Shukron, Ariella, Abulibdeh, Abdulsalam, Garfinkel, Benjamin P., Dweik, Dima, Kanaan, Moein, Camats, Núria, Flück, Christa, Renbaum, Paul, Levy-Lahad, Ephrat
Publicado em 2014

FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells

Por Avitzour, Michal, Mor-Shaked, Hagar, Yanovsky-Dagan, Shira, Aharoni, Shira, Altarescu, Gheona, Renbaum, Paul, Eldar-Geva, Talia, Schonberger, Oshrat, Levy-Lahad, Ephrat, Epsztejn-Litman, Silvina, Eiges, Rachel
Publicado no Stem Cell Reports (2014)

Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations

Por Zeevi, David A., Altarescu, Gheona, Weinberg-Shukron, Ariella, Zahdeh, Fouad, Dinur, Tama, Chicco, Gaya, Herskovitz, Yair, Renbaum, Paul, Elstein, Deborah, Levy-Lahad, Ephrat, Rolfs, Arndt, Zimran, Ari
Publicado no J Clin Invest (2015)

Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome

Por Pierce, Sarah B., Walsh, Tom, Chisholm, Karen M., Lee, Ming K., Thornton, Anne M., Fiumara, Agata, Opitz, John M., Levy-Lahad, Ephrat, Klevit, Rachel E., King, Mary-Claire
Publicado em 2010

p53-dependent control of transactivation of the Pen2 promoter by presenilins

Por Dunys, Julie, Sevalle, Jean, Giaime, Emilie, Pardossi-Piquard, Raphaëlle, Vitek, Michael P., Renbaum, Paul, Levy-Lahad, Ephrat, Zhang, Yun-wu, Xu, Huaxi, Checler, Frédéric, da Costa, Cristine Alves
Publicado em 2009

Parkin acts as a transcription factor modulating presenilin-1 and presenilin-2 promoter transactivations

Por Duplan, Eric, Sévalle, Jean, Viotti, Julien, Goiran, Thomas, Bauer, Charlotte, Renbaum, Paul, Levy-Lahad, Ephrat, Gautier, Clément A, Corti, Olga, Leroudier, Nathalie, Checler, Frédéric, da Costa, Cristine Alves
Publicado em 2013